Evidence map›Paper›PMID 27778160›Full record

ArticleJournal of neurology2017

New evidence for involvement of ESR1 gene in susceptibility to Chinese migraine.

Xingkai An, Jie Fang, Qing Lin, Congxia Lu, Qilin Ma, Hongli Qu

Abstract read
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In one paragraph

Article in Journal of neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Sex-Specific Physiology and Cardiovascular Disease.Advances in experimental medicine and biology
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Xingkai AnDepartment of Neurology, The First Affiliated Hospital of Xiamen University, Xiamen, China.
Jie FangDepartment of Neurology, The First Affiliated Hospital of Xiamen University, Xiamen, China.
Qing LinDepartment of Neurology, The First Affiliated Hospital of Xiamen University, Xiamen, China.
Congxia LuDepartment of Neurology, The First Affiliated Hospital of Xiamen University, Xiamen, China.
Qilin MaDepartment of Neurology, The First Affiliated Hospital of Xiamen University, Xiamen, China. xmqilinma@hotmail.com.
Hongli QuDepartment of Neurology, The First Affiliated Hospital of Xiamen University, Xiamen, China. xmhongliqu@hotmail.com.
First Affiliated Hospital of Xiamen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Migraine is a common and disabling nervous system disease with a significant genetic predisposition. The sex hormones play an important role in the pathogenesis of migraine. However, the conclusions of the previous genetic relation studies are conflicting. The aim of this study is to determine whether variants in genes involved in estrogen receptor and estrogen hormone metabolism are related to Chinese migraine. By employing a case-control approach, 8 SNPs in the ESR1, ESR2, and CYP19A1 genes are studied in a cohort of 494 migraine cases and 533 controls. In addition, genotyping is performed using Sequenom MALDI-TOF mass spectrometry iPLEX platform. Univariate and multivariate analyses are carried out by logistic regression. The corresponding haplotypes are studied with the Haploview software and gene-gene interaction is assessed using the Generalized Multifactor Dimensionality Reduction (GMDR) analysis. There are significant differences in allelic distributions for rs2234693 and rs9340799 in ESR1 gene between patients with migraine and control subjects. Univariate logistic analysis shows that rs2234693 and rs9340799 are risk factors for migraine, but multivariate analysis reveals that only rs2234693 is significant associated with migraine. In the subgroup analysis, rs2234693 in ESR1 gene is found associated with menstrually related migraine. Further haplotypic analysis shows that rs2234693-rs9340799 TA haplotype serves as risk haplotype for migraine. The GMDR analysis identifies rs2234693 in ESR1 alone to be a crucial candidate in migraine susceptibility. This study is in agreement with the previous studies that variants in the ESR1 gene are associated with migraine suggesting that it plays a role in the migraine process.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAdultAromataseAsian PeopleCase-Control StudiesChinaEstrogen Receptor alphaEstrogen Receptor betaFemaleGene FrequencyGenetic Association StudiesGenotyping TechniquesHumansLogistic ModelsMaleAromataseCYP19A1 protein, humanESR1 protein, humanESR2 protein, humanEstrogen Receptor alphaEstrogen Receptor betaChinaCYP19A1ESR1ESR2MigrainePolymorphism

Identifiers

PMID27778160
OpenAlexW2536091901

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.